-
1
-
-
4243475879
-
Quantitative and qualitative disorders of fibrinogen
-
R. et al. Hoffman. New York: Churchill Livingstone
-
Martinez J. Quantitative and qualitative disorders of fibrinogen. Hoffman R.et al. Hematology. 3rd Ed. 2000;1924-1936 Churchill Livingstone, New York.
-
(2000)
Hematology 3rd Ed.
, pp. 1924-1936
-
-
Martinez, J.1
-
2
-
-
0011233567
-
-
http://www.geht.org/pages/database_fibrino_uk.html.
-
-
-
-
3
-
-
0034078071
-
Identification of a dysfibrinogen, the substitution of γ308Asn (AAT) to Lys (AAG), using coagulation tests, immunoblot analysis, and allele-specific polymerase chain reaction
-
Terasawa F., Fujita K., Tozuka M., Ota H., Katsuyama T., Okumura N. Identification of a dysfibrinogen, the substitution of γ308Asn (AAT) to Lys (AAG), using coagulation tests, immunoblot analysis, and allele-specific polymerase chain reaction. Clin. Chim. Acta. 295:2000;77-85.
-
(2000)
Clin. Chim. Acta
, vol.295
, pp. 77-85
-
-
Terasawa, F.1
Fujita, K.2
Tozuka, M.3
Ota, H.4
Katsuyama, T.5
Okumura, N.6
-
4
-
-
0021070892
-
Fibrinogen Tokyo II: An abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules
-
Matsuda M., Baba M., Morimoto K., Nakamikawa K. Fibrinogen Tokyo II: an abnormal fibrinogen with an impaired polymerization site on the aligned DD domain of fibrin molecules. J. Clin. Invest. 72:1983;1034-1041.
-
(1983)
J. Clin. Invest.
, vol.72
, pp. 1034-1041
-
-
Matsuda, M.1
Baba, M.2
Morimoto, K.3
Nakamikawa, K.4
-
5
-
-
0024421560
-
Fibrinogen Baltimore IV: Congenital dysfibrinogenemia with a γ275 (Arg→Cys) substitution
-
Schmelzer C.H., Ebert R.F., Bell W.R. Fibrinogen Baltimore IV: congenital dysfibrinogenemia with a γ275 (Arg→Cys) substitution. Thromb. Res. 56:1989;307-316.
-
(1989)
Thromb. Res.
, vol.56
, pp. 307-316
-
-
Schmelzer, C.H.1
Ebert, R.F.2
Bell, W.R.3
-
6
-
-
0000792704
-
Two abnormal fibrinogens designated as Osaka II and Morioka with a hitherto unidentified amino acid substitution; γ Arg 275 by Cys
-
abstract
-
Terukina S., Matsuda M., Yoshida N., Yamazaki N., Takeda Y., Takano T. Two abnormal fibrinogens designated as Osaka II and Morioka with a hitherto unidentified amino acid substitution; γ Arg 275 by Cys. Thromb. Haemost. 58:1987;515. [abstract].
-
(1987)
Thromb. Haemost.
, vol.58
, pp. 515
-
-
Terukina, S.1
Matsuda, M.2
Yoshida, N.3
Yamazaki, N.4
Takeda, Y.5
Takano, T.6
-
7
-
-
0023860974
-
An apparently higher molecular weight γ-chain variant in a new congenital abnormal fibrinogen Tochigi characterized by the replacement of γ arginine-275 by cysteine
-
Yoshida N., Ota K., Moroi M., Matsuda M. An apparently higher molecular weight γ-chain variant in a new congenital abnormal fibrinogen Tochigi characterized by the replacement of γ arginine-275 by cysteine. Blood. 71:1988;480-487.
-
(1988)
Blood
, vol.71
, pp. 480-487
-
-
Yoshida, N.1
Ota, K.2
Moroi, M.3
Matsuda, M.4
-
8
-
-
0023755597
-
Substitution of γ Arg-275 by Cys in an abnormal fibrinogen, "Fibrinogen Osaka II"
-
Terukina S., Matsuda M., Hirata H.et al. Substitution of γ Arg-275 by Cys in an abnormal fibrinogen, "Fibrinogen Osaka II" J. Biol. Chem. 263:1988;13579-13587.
-
(1988)
J. Biol. Chem.
, vol.263
, pp. 13579-13587
-
-
Terukina, S.1
Matsuda, M.2
Hirata, H.3
-
9
-
-
0028092830
-
Fibrinogen Milano V: A congenital dysfibrinogenemia with a γ275→Cys substitution
-
Steinmann C., Bögli C., Jungo M.et al. Fibrinogen Milano V: a congenital dysfibrinogenemia with a γ275→Cys substitution. Blood Coagul. Fibrinolysis. 5:1994;463-471.
-
(1994)
Blood Coagul. Fibrinolysis
, vol.5
, pp. 463-471
-
-
Steinmann, C.1
Bögli, C.2
Jungo, M.3
-
10
-
-
0029026342
-
Abnormal polymerization and normal binding of plasminogen and t-PA in three new dysfibrinogenaemias: Barcelona III and IV (γArg275→His) and Villajoyosa (γArg275→Cys)
-
Borrell M., Garí M., Coll I.et al. Abnormal polymerization and normal binding of plasminogen and t-PA in three new dysfibrinogenaemias: Barcelona III and IV (γArg275→His) and Villajoyosa (γArg275→Cys). Blood Coagul. Fibrinolysis. 6:1995;198-206.
-
(1995)
Blood Coagul. Fibrinolysis
, vol.6
, pp. 198-206
-
-
Borrell, M.1
Garí, M.2
Coll, I.3
-
11
-
-
0028877613
-
Familial dysfibrinogenemia and thrombophilia
-
Haverkate F., Samama M. Familial dysfibrinogenemia and thrombophilia. Thromb. Haemost. 73:1995;151-161.
-
(1995)
Thromb. Haemost.
, vol.73
, pp. 151-161
-
-
Haverkate, F.1
Samama, M.2
-
12
-
-
0032934525
-
Fibrinogen Matsumoto III: A variant with γ275 Arg→Cys (CGC→TGC)-comparison of fibrin polymerization properties with those of Matsumoto I (γ364 Asp→His) and Matsumoto II (γ308 Asn→Lys)
-
Terasawa F., Okumura N., Higuchi Y.et al. Fibrinogen Matsumoto III: a variant with γ275 Arg→Cys (CGC→TGC)-comparison of fibrin polymerization properties with those of Matsumoto I (γ364 Asp→His) and Matsumoto II (γ308 Asn→Lys). Thromb. Haemost. 81:1999;763-766.
-
(1999)
Thromb. Haemost.
, vol.81
, pp. 763-766
-
-
Terasawa, F.1
Okumura, N.2
Higuchi, Y.3
-
13
-
-
0033853934
-
Fibrinogen Bellingham: A γ-chain R275C substitution and a β-promoter polymorphism in a thrombotic member of an asymptomatic family
-
Linenberger M.L., Kindelan J., Bennett R.L., Reiner A.P., Côté H.C.F. Fibrinogen Bellingham: a γ-chain R275C substitution and a β-promoter polymorphism in a thrombotic member of an asymptomatic family. Am. J. Hematol. 64:2000;242-250.
-
(2000)
Am. J. Hematol.
, vol.64
, pp. 242-250
-
-
Linenberger, M.L.1
Kindelan, J.2
Bennett, R.L.3
Reiner, A.P.4
Côté, H.C.F.5
-
14
-
-
0033623697
-
Coexisting dysfibrinogenemia (γR275C) and factor V Leiden deficiency associated with thromboembolic disease (fibrinogen Cedar Rapids)
-
Siebenlist K.R., Mosesson M.W., Meh D.A., DiOrio J.P., Albrecht R.M., Olson J.D. Coexisting dysfibrinogenemia (γR275C) and factor V Leiden deficiency associated with thromboembolic disease (fibrinogen Cedar Rapids). Blood Coagul. Fibrinolysis. 11:2000;293-304.
-
(2000)
Blood Coagul. Fibrinolysis
, vol.11
, pp. 293-304
-
-
Siebenlist, K.R.1
Mosesson, M.W.2
Meh, D.A.3
DiOrio, J.P.4
Albrecht, R.M.5
Olson, J.D.6
-
16
-
-
0032189655
-
γ-chain dysfibrinogenemias: Molecular structure-function relationships of naturally occurring mutations in the γ-chain of human fibrinogen
-
Côté H.C.F., Lord S.T., Pratt K.P. γ-chain dysfibrinogenemias: molecular structure-function relationships of naturally occurring mutations in the γ-chain of human fibrinogen. Blood. 92:1998;2195-2212.
-
(1998)
Blood
, vol.92
, pp. 2195-2212
-
-
Côté, H.C.F.1
Lord, S.T.2
Pratt, K.P.3
-
17
-
-
0030848486
-
Crystal structures of fragment D from human fibrinogen and its crosslinked counterpart from fibrin
-
Spraggon G., Everse S.J., Doolitle R.F. Crystal structures of fragment D from human fibrinogen and its crosslinked counterpart from fibrin. Nature. 389:1997;455-462.
-
(1997)
Nature
, vol.389
, pp. 455-462
-
-
Spraggon, G.1
Everse, S.J.2
Doolitle, R.F.3
-
18
-
-
0032537486
-
Crystal structure of fragment double-D from human fibrin with two different bound ligands
-
Everse S.J., Spraggon G., Veerapandian L., Marcia R., Doolittle R.F. Crystal structure of fragment double-D from human fibrin with two different bound ligands. Biochemistry. 37:1998;8637-8642.
-
(1998)
Biochemistry
, vol.37
, pp. 8637-8642
-
-
Everse, S.J.1
Spraggon, G.2
Veerapandian, L.3
Marcia, R.4
Doolittle, R.F.5
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